The Effects of Prenatal Prescription Medication Exposure on Neonatal Abstinence Syndrome
Loading...
Authors
Donelle, Jessy
Date
Type
thesis
Language
eng
Keyword
Neonatal Abstinence Syndrome , Methadone , Buprenorphine , Expression , Growth Curves , Symptom
Alternative Title
Abstract
Background: The increased occurrence of neonatal abstinence syndrome (NAS) is a major public health concern within Canada and the United States. NAS is a drug withdrawal syndrome caused by the abrupt cessation of prolonged prenatal exposure to opioids. Because of the increasing number of infants affected with NAS and subsequent increased utilization of hospital resources for NAS, research to improve NAS definition, measurement, and management is needed. This study aims to describe the presentation of NAS in neonates prenatally exposed to buprenorphine vs. methadone.
Methods: We conducted a prospective cohort study of pregnant women with opioid use disorder and their neonates. Women were treated with buprenorphine or methadone based on clinical indicators and patient preference. Neonates were assessed using the 31-item Finnegan scale and scored every four hours, increasing to every two hours if NAS pharmacotherapy was initiated. Differences in NAS symptoms were compared among 34 buprenorphine-exposed neonates and 43 methadone-exposed neonates prior to and following NAS pharmacotherapy initiation were statistically assessed. Individual growth curve models (IGC) were applied to the Finnegan score data, adjusted for confounders, and NAS trajectories were plotted by prenatal exposure to buprenorphine or methadone.
Results: Prior to NAS pharmacotherapy initiation, four NAS symptoms were observed significantly more often in buprenorphine exposed neonates compared to methadone exposed neonates: continuous high pitched crying (76.5% vs. 32.6%), hyperactive Moro reflex (47.1% vs. 23.3%), nasal stuffiness (42.4% vs. 15.9%), and loose stools (50.0% vs. 23.3 Furthermore, we were able to successfully apply an IGC approach to modeling change trajectories to repeated Finnegan score data. Differences in NAS progression by prenatal opioid agonist therapy exposure were identified in neonates who required NAS pharmacotherapy.
Conclusion: This is one of the first studies to investigate NAS symptom expression by prenatal opioid agonist therapy exposure to buprenorphine and methadone. This study will provide a resource for other researchers to apply these novel procedures which have not been previously used in pediatric research. The findings from this study provide insight into how these two prenatal medications affect NAS symptom expression and NAS progression allowing healthcare professionals to improve NAS definition, measurement, and management.
Description
Citation
Publisher
License
Queen's University's Thesis/Dissertation Non-Exclusive License for Deposit to QSpace and Library and Archives Canada
ProQuest PhD and Master's Theses International Dissemination Agreement
Intellectual Property Guidelines at Queen's University
Copying and Preserving Your Thesis
This publication is made available by the authority of the copyright owner solely for the purpose of private study and research and may not be copied or reproduced except as permitted by the copyright laws without written authority from the copyright owner.
ProQuest PhD and Master's Theses International Dissemination Agreement
Intellectual Property Guidelines at Queen's University
Copying and Preserving Your Thesis
This publication is made available by the authority of the copyright owner solely for the purpose of private study and research and may not be copied or reproduced except as permitted by the copyright laws without written authority from the copyright owner.
